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Home โ€บ Jobs โ€บ Lagos , Ogun โ€บ Senior Pharmaceutical Quality Assurance Manager

Senior Pharmaceutical Quality Assurance Manager

Sagar Vitaceuticals Nigeria Limited  ยท Pharmaceuticals

Full Time Lagos , Ogun
Lagos , Ogun
200,000 - 300,000/month
Deadline: 8 September 2026
Posted June 9, 2026

Key Responsibilities

The position oversees the efficient management and execution of laboratory operations, ensuring adherence to established protocols and regulatory standards. Key responsibilities include maintaining equipment functionality, documenting experimental procedures, and managing inventory of supplies and reagents. Additionally, the role requires collaboration with cross-functional teams to support research initiatives, analyze data, and report findings accurately. Candidates must possess a degree in a scientific discipline, practical experience in a laboratory setting, and proficiency in relevant software tools. Strong organizational skills, attention to detail, and the ability to work in a fast-paced environment are essential.

Support the oversight and coordination of routine Quality Control laboratory operations on a daily basis.

Oversee the execution of chemical, microbiological, and physical testing procedures for raw materials, packaging materials, in-process samples, and finished products.

Deliver laboratory results with promptness, ensuring accurate and timely analysis and reporting.

To ensure adherence to production and release schedules, oversee and synchronize laboratory operations efficiently.

Ensures adherence to established quality standards and regulatory requirements throughout all operational processes. Conducts routine audits, inspections, and assessments to identify non-compliance issues and implement corrective actions. Collaborates with cross-functional teams to maintain compliance documentation, track performance metrics, and drive continuous improvement initiatives. Requires meticulous attention to detail, strong analytical skills, and proficiency in quality management systems. Prior experience in quality assurance or regulatory compliance within a regulated industry is essential.

Maintain adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs), and all applicable regulatory standards.

Facilitate both internal and external audits, as well as regulatory inspections, to ensure compliance with established standards and requirements.

Ensure strict compliance with established quality systems and laboratory best practices to maintain operational excellence and regulatory standards.

Investigate deviations, out-of-specification (OOS) results, and out-of-trend (NOT) occurrences as part of comprehensive assessments.

Responsibilities include compiling, organizing, and maintaining accurate records while ensuring compliance with established standards. This role requires meticulous attention to detail to produce clear, concise reports that effectively communicate key information to stakeholders. Additionally, the position demands proficiency with documentation tools and software to streamline processes and enhance data integrity. Strong analytical and communication skills are essential to interpret data accurately and present findings in a structured manner. A commitment to maintaining up-to-date documentation and adhering to reporting protocols is critical for this role.

Examine analytical reports, laboratory documentation, certificates of analysis, and test records to ensure accuracy and compliance with established standards.

Maintain meticulous documentation, organize files appropriately, and retain records in strict adherence to all applicable regulatory requirements.

Collaborate on the development and compilation of quality metrics, as well as management reports.

The Equipment & Method Management role entails overseeing the maintenance, calibration, and documentation of all laboratory equipment to ensure compliance with regulatory standards and operational efficiency. This position requires a meticulous individual with a strong background in equipment validation, method development, and adherence to Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP). Key responsibilities include implementing preventative maintenance schedules, troubleshooting technical issues, and ensuring that all methodologies adhere to industry best practices. Additionally, the role involves training staff on proper equipment usage, updating standard operating procedures (SOPs), and maintaining detailed records for audits and inspections.

Provide oversight for the calibration, qualification, and maintenance processes of all laboratory instruments and equipment to ensure compliance with established standards and operational efficiency.

Conduct activities related to the validation, verification, and transfer of analytical methods to ensure their reliability and accuracy.

Maintain an adequate supply of laboratory reagents, standards, and consumables to support uninterrupted operations.

Leads, motivates, and guides a team to achieve organizational goals through clear direction and support. Develops team members by identifying strengths, addressing skill gaps, and fostering professional growth opportunities. Ensures adherence to company policies, performance standards, and project timelines while maintaining open communication channels. Collaborates with cross-functional departments to align team objectives with broader business strategies. Monitors progress, provides constructive feedback, and resolves conflicts to maintain a high-performing and cohesive team dynamic.

Oversee and provide guidance to quality control analysts as well as laboratory personnel, ensuring their professional development and adherence to established standards.

Support the facilitation of staff training initiatives and the enhancement of competency development programs.

Promote a culture of quality, safety, and continuous improvement.

We are seeking a dedicated professional to oversee safety protocols and drive continuous improvement initiatives within our organization. The ideal candidate will ensure compliance with all safety regulations, implement robust safety measures, and foster a culture of proactive risk management. Responsibilities include conducting regular safety audits, analyzing incident reports to identify trends, and developing corrective actions to mitigate future risks. Additionally, the role involves collaborating with cross-functional teams to integrate safety best practices into daily operations, leading training sessions to enhance employee awareness, and monitoring performance metrics to track progress. Proficiency in safety management systems and a commitment to continuous improvement methodologies are essential for success in this position.

Maintain adherence to established laboratory safety protocols and environmental regulations.

Review operational workflows within the Quality Control department to uncover potential avenues for enhancement and efficiency gains.

Facilitate the execution of CAPA (Corrective and Preventive Actions) initiatives to enhance operational efficiency and compliance standards.

Interested candidates who meet the required qualifications are encouraged to submit their CV via email to recruitment@svnl.in, with the position title specified in the subject line.

Qualifications

BA/BSc/HND , MBA/MSc/MA

Experience Required

6 - 10 years

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